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Plasma ascorbic acid concentrations in prevalent patients with end-stage renal disease on hemodialysis
William D Sirover1, Yuguan Liu2, Amanda Logan3
1Division of Nephrology, Department of Medicine, Cooper Medical School of Rowan University, Camden, New Jersey.
Insights
Hemodialysis significantly lowers vitamin C levels in patients with end-stage renal disease. Supplementation is crucial for maintaining adequate ascorbic acid (AA) concentrations in this population.
Area of Science:
- Nephrology
- Nutritional Science
- Biochemistry
Background:
- Patients with end-stage renal disease (ESRD) often exhibit vitamin C deficiency.
- Hemodialysis (HD) is a common treatment for ESRD, but its impact on vitamin C levels is not fully understood.
- Understanding factors influencing vitamin C status in ESRD patients is critical for optimizing health outcomes.
Purpose of the Study:
- To determine the prevalence of vitamin C (ascorbic acid [AA]) deficiency in ESRD patients.
- To assess the effect of supplemental AA on plasma AA concentrations.
- To identify factors affecting plasma AA concentrations in ESRD patients undergoing HD.
Main Methods:
- Study 1: Compared plasma AA concentrations in patients with low vs. high pre-HD levels during and after HD treatment.
- Study 2: Analyzed demographic and lifestyle factors associated with plasma AA concentrations in 203 adult HD patients.
- Plasma AA levels, supplement use, and dietary intake were measured.
Main Results:
- Hemodialysis caused a significant mean decrease of 60% in plasma AA concentrations.
- Patients taking AA supplements had significantly higher median pre-HD plasma AA concentrations (50.6 μM) compared to non-supplement users (15.7 μM).
- Supplement use, advanced age, and diabetes mellitus were linked to higher pre-HD plasma AA levels (≥30 μM).
Conclusions:
- Hemodialysis treatment leads to substantial depletion of plasma ascorbic acid.
- Vitamin C supplementation is effective in increasing and maintaining higher plasma AA concentrations in ESRD patients.
- Supplement use and certain patient characteristics influence vitamin C status in this population.
Objective:
To determine the prevalence of vitamin C (ascorbic acid [AA]) deficiency in patients with end-stage renal disease, the effect of supplemental AA on plasma AA concentrations, and the extrinsic and intrinsic factors that affect plasma AA concentrations in this patient population.
Design:
In study 1, we compared the effect of hemodialysis (HD) on plasma AA concentrations between patients with low and high pre-HD AA concentrations. In study 2, we analyzed kinetic and nonkinetic factors for their association with increased plasma AA concentrations in patients on maintenance HD. Study 1 was performed in a single outpatient HD clinic in Cherry Hill, New Jersey. Study 2 was performed in 4 outpatient HD clinics in Southern New Jersey.
Subjects And Intervention:
In study 1, we collected plasma samples from 8 adult patients on maintenance HD at various time points around their HD treatment and assayed them for AA concentration. In study 2, we enrolled 203 adult patients and measured pre-HD plasma AA concentrations. We ascertained supplemental AA use and assessed dietary AA intake.
Main Outcome Measure:
In study 1, plasma AA concentrations were compared during the intradialytic and interdialytic period. In study 2, pre-HD plasma AA concentrations were correlated with supplement use and demographic factors.
Results:
Study 1 showed that over the course of a single HD treatment, the plasma AA concentration decreased by a mean (±standard deviation) of 60% (±6.6). In study 2, the median pre-HD plasma AA concentration was 15.7 μM (interquartile range, 8.7-66.8) in patients who did not take a supplement and 50.6 μM (interquartile range, 25.1-88.8) in patients who did take a supplement (P < .001). Supplement use, increasing age, and diabetes mellitus were associated with a pre-HD plasma AA concentration ≥30 μM.
Conclusion:
HD depletes plasma AA concentrations, and AA supplementation allows patients to achieve higher plasma AA concentrations.
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